Search research articles
Contact Us
Filters
Showing results (131-140 of 377) with videos related to
Page
of 38
Sort By:
Journal De Genetique Humaine
|
September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]
C Stoll, M P Roth, J M Levy
Genetic Counseling (Geneva, Switzerland)
|
July 17, 1998
Wiedemann-Rautenstrauch syndrome. A case report and review of the literature
C Stoll, F Labay, J Geisert, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Familial cylindromatosis
C Stoll, Y Alembik, A Wilk, et al.
Clinical Genetics
|
January 1, 1976
An unusual partial trisomy 13
C Stoll, J Messer, S Weitzenblum, et al.
Archives Francaises De Pediatrie
|
October 1, 1988
[Radiologic case of the month. Pneumatocele on infected intrapulmonary hematoma]
Y Alembik, L Donato, C Roy, et al.
Annales De Genetique
|
January 1, 1997
De novo trisomy 22 due to an extra 22Q-chromosome
C Stoll, P Medeiros, H Pécheur, et al.
Birth Defects Original Article Series
|
January 1, 1976
Usefulness of chromosome catalog in delineating new syndromes
D S Borgaonkar, Y E Lacassie, C Stoll
Laryngo- Rhino- Otologie
|
July 27, 2000
[Speech improvement with velopharyngoplasty in patients with lip-jaw-palate clefts]
C Stoll, M Hochmuth, M Merting, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
August 31, 2000
Refinement of velopharyngoplasty in patients with cleft palate by covering the pharyngeal flap with nasal mucosa from the velum
C Stoll, M Hochmuth, P Meister, et al.
Advances in Experimental Medicine and Biology
|
February 23, 1999
The influence of CD44 splice variants to the outcome of patients with oral squamous cell carcinoma
C Stoll, G Baretton, F Soost, et al.
Page
of 38
Search research articles
Search
Showing results (131-140 of 377) with videos related to
Sort By:
Page
of 38
Journal De Genetique Humaine
|
September 1, 1980
[Articular contracture with dwarfism and normal intelligence: a new autosomal dominant familial syndrome]
C Stoll, M P Roth, J M Levy
Genetic Counseling (Geneva, Switzerland)
|
July 17, 1998
Wiedemann-Rautenstrauch syndrome. A case report and review of the literature
C Stoll, F Labay, J Geisert, et al.
Genetic Counseling (Geneva, Switzerland)
|
August 4, 2004
Familial cylindromatosis
C Stoll, Y Alembik, A Wilk, et al.
Clinical Genetics
|
January 1, 1976
An unusual partial trisomy 13
C Stoll, J Messer, S Weitzenblum, et al.
Archives Francaises De Pediatrie
|
October 1, 1988
[Radiologic case of the month. Pneumatocele on infected intrapulmonary hematoma]
Y Alembik, L Donato, C Roy, et al.
Annales De Genetique
|
January 1, 1997
De novo trisomy 22 due to an extra 22Q-chromosome
C Stoll, P Medeiros, H Pécheur, et al.
Birth Defects Original Article Series
|
January 1, 1976
Usefulness of chromosome catalog in delineating new syndromes
D S Borgaonkar, Y E Lacassie, C Stoll
Laryngo- Rhino- Otologie
|
July 27, 2000
[Speech improvement with velopharyngoplasty in patients with lip-jaw-palate clefts]
C Stoll, M Hochmuth, M Merting, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
August 31, 2000
Refinement of velopharyngoplasty in patients with cleft palate by covering the pharyngeal flap with nasal mucosa from the velum
C Stoll, M Hochmuth, P Meister, et al.
Advances in Experimental Medicine and Biology
|
February 23, 1999
The influence of CD44 splice variants to the outcome of patients with oral squamous cell carcinoma
C Stoll, G Baretton, F Soost, et al.
Page
of 38